meddevicedb.com FDA Device Reference

SHARP DISPOSAL CONTAINERS WALL SAFE

K941664 Class II Traditional
Decision Date
1994-05-23
Sponsor / Applicant
Bemis Mfg. Co.

Technical Specification

510(k) Submission ID K941664
Product Code MMK
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5570
Decision Date 1994-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHARP DISPOSAL CONTAINERS WALL SAFE received FDA 510(k) clearance under submission number K941664, sponsored by Bemis Mfg. Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1994-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code MMK and 21 CFR 880.5570, within the General Hospital review panel as a Class II device.